Nucleic acids isolated in neuroblastoma

ABSTRACT

There are disclosed a nucleic acid whose expression is enhanced in human neuroblastoma with unfavorable prognosis based on comparison between human neuroblastoma with favorable prognosis and human neuroblastoma with unfavorable prognosis, the nucleic acid comprising any one of base sequences set forth in SEQ ID NO:1 to NO:69 in the Sequence Listing, a nucleic acid comprising a portion of any of those base sequences, and an isolated nucleic acid capable of hybridizing to a complementary base sequence of the foregoing under stringent conditions. It discloses gene sequences relating to favorable or unfavorable prognosis of neuroblastoma and will enable the provision of their genetic information and the diagnosis of favorable or unfavorable prognosis.

CROSS-REFERENCED APPLICATIONS

This application is a National phase of International Application PCT/JP02/05294, filed May 30, 2002, which designated the U.S. and that International Application was not published under PCT Article 21(2) in English.

TECHNICAL FIELD

This invention relates to nucleic acids whose expression is enhanced in human neuroblastoma with unfavorable prognosis based on comparison between human neuroblastoma with favorable prognosis and human neuroblastoma with unfavorable prognosis.

BACKGROUND ART

(Tumorgenesis and Genes)

Individual tumors exhibit distinct characteristic natures, and their biological properties are not necessarily identical even though the basic principle of oncogenesis is the same. Rapid advances in the understanding of cancer from a molecular biological and molecular genetic perspective in recent year have opened the way to an explanation of oncogenesis and tumor cell biology on the genetic level.

(Neuroblastomas)

Neuroblastoma is a pediatric cancer occurring in sympathetic gangliocytes and adrenal medullary cells which originate from cells of the peripheral sympathetic nervous system. Of these sympathetic nervous system cells, neural crest cells in the initial stage of development migrate to the abdomen, differentiating and maturing at sites where sympathetic ganglia are formed. Some of these cells migrate further to the adrenal bodies, penetrating through the adrenal cortex which is already in the process of formation, and reaching the medulla and forming medullary substance there. The neural crest cells also serve as a source of other peripheral nerve cells, differentiating into dorsal root ganglia (sensory nerves), skin pigment cells, thyroid C cells, some pulmonary cells, intestinal gangliocytes, and the like.

(Prognosis for Neuroblastoma)

Neuroblastoma is characterized by a varied clinical profile (Nakagawara, Shinkeigashu no Hassei to Sono Bunshi Kiko [Neuroblastoma Development and Molecular Mechanism], Shoni Naika 30, 143, 1998). For example, neuroblastomas occurring at less than one year of age have very favorable prognosis, with the majority undergoing differentiation and cell death, and spontaneous regression. Currently, most neuroblastomas discovered by a positive result in the commonly performed mass screening of 6-month-old infant urine are of the type which tend to undergo this spontaneous regression. On the other hand, neuroblastomas occurring at age 1 or higher are highly malignant and lead to death of the infant in the majority of cases. It is also hypothesized that a somatic mutation occurs in highly malignant neuroblastomas in infants older than one year of age, which are of monoclonal nature, whereas in naturally regressing neuroblastomas, the genetic mutation remains at only a germline mutation. See Knudson AG, et al.: Regression of neuroblastoma IV-S: A genetic hypothesis, N. Engl. J. Med. 302, 1254 (1980)).

(Tumor Markers which Allow the Diagnosis of Prognosis for Neuroblastoma)

With recent advances in molecular biology research, it has become clear that expression of the high affinity nerve growth factor (NGF) receptor TrkA is closely connected with control of differentiation and cell death. See Nakagawara A., The NGF story and neuroblastoma, Med. Pediatr. Oncol., 31, 113 (1998). Trk is a membrane-spanning receptor, existing as the three main types, Trk-A, -B and -C. These Trk family receptors play an important role in specific nerve cell differentiation and survival in the central nervous and peripheral nervous systems. See Nakagawara, et al., Shinkeigasaiboushu ni Okeru Neurotrophin Juyoutai no Hatsugen to Yogo [Expression of Neurotrophin Receptors and Prognosis in Neuroblastoma], Shoni Geka (Pediatric Surgery), 29:425-432, 1997. The survival and differentiation of tumor cells is controlled by signals from Trk tyrosine kinase and Ret tyrosine kinase. In particular, the role of TrkA receptor is most significant, with TrkA expression being notably high in neuroblastomas with favorable prognosis, and its signals exerting a powerful control over survival and differentiation of tumor cells, and cell death (apoptosis). In neuroblastomas with unfavorable prognosis, on the other hand, TrkA expression is significantly suppressed, while tumor development is aided by a mechanism in which survival is promoted by signals from TrkB and Ret.

It has become clear that amplification of the neural oncogene N-myc has become clearly associated with the prognosis of neuroblastoma. See Nakagawara, Nou-shinkeishuyo no Tadankai Hatsugan [Multistage Oncogenesis of Cerebral and Neural Tumors], Molecular Medicine, 364, 366(1999). This gene, first cloned in neuroblastoma, is ordinarily only present in a single copy per haploid set in normal cells and neuroblastomas with favorable prognosis, whereas it has been found to be amplified several dozen times in neuroblastomas with unfavorable prognosis.

Up till the present time, however, no oncogene other than N-myc is known to be expressed in neuroblastomas, and absolutely no genetic information other than that of N-myc has been known in relation to favorable or unfavorable prognosis.

DISCLOSURE OF THE INVENTION

This invention has been accomplished in light of the circumstances described above, and its object is to identify the gene sequences which are related to favorable or unfavorable prognosis of neuroblastoma, and to allow the provision of their genetic information as well as the diagnosis for favorable or unfavorable prognosis.

As a result of conducting diligent research, the present inventors have examined the prognoses of neuroblastomas and have succeeded in constructing cDNA libraries from both clinical tissues with favorable prognosis and with unfavorable prognosis. Approximately 2400 clones were respectively obtained from these two types of cDNA libraries and were classified according to the prognosis of neuroblastoma (whether favorable or unfavorable).

Moreover, the present inventors found that the expression of a considerable number of the genes is enhanced only in clinical tissues of neuroblastoma with unfavorable prognosis among the classified genes.

Based on such knowledge, the present inventors have succeeded in providing base sequence information for the detection and cloning of the genes only expressed in clinical tissues with unfavorable prognosis.

Furthermore, based on the aforementioned base sequence information on the regions it has been made possible to carry out the method for detection of prognosis and to design tumor markers which can be used therefor, and this invention has thereupon been completed.

Specifically, this invention aims at providing a nucleic acid whose expression is enhanced in human neuroblastoma with unfavorable prognosis based on comparison between human neuroblastoma with favorable prognosis and human neuroblastoma with unfavorable prognosis, the nucleic acid comprising any one of base sequences set forth in SEQ ID NO:1 to NO:69 in the Sequence Listing as well as providing a nucleic acid comprising a portion of the base sequence. This invention also provides an isolated nucleic acid characterized in that it hybridizes to the nucleic acid described above or its complementary nucleic acid under stringent conditions.

The nucleic acids of this invention are those whose expression is enhanced in human neuroblastoma with unfavorable prognosis based on comparison between human neuroblastoma with favorable prognosis and human neuroblastoma with unfavorable prognosis and those nucleic acids are characterized by their capabilities of being used in the diagnosis for prognosis of human neuroblastoma. The preferred nucleic acid for this purpose is a nucleic acid comprising the base sequence set forth in SEQ ID NO:21 or the base sequence set forth in SEQ ID NO:64 in the Sequence Listing or a nucleic acid related thereto (e.g., a nucleic acid comprising a portion of the base sequence).

This invention also provides a diagnostic agent for the detection of a neurological disease characterized by containing at least one nucleic acid comprising a portion or the whole of a base sequence set forth in SEQ ID NO:1 to SEQ ID NO:69 in the Sequence Listing. Specifically, such tumor detection diagnostic agents include DNA chips and microarrays both of which are produced using the above-mentioned nucleic acids, for example. Accordingly, this invention also provides a microarray composition characterized by containing plural numbers of nucleic acids comprising a portion or the whole of the base sequence set forth in SEQ ID NO:1 to SEQ ID NO:69 in the Sequence Listing. Preferably, such composition comprises all the nucleic acids, i.e., a total of 69 nucleic acids each of which comprises a portion or the whole of a base sequence set forth in SEQ ID NO:1 to SEQ ID NO:69 in the Sequence Listing.

Further according to this invention there is provided an isolated nucleic acid which is DNA characterized by hybridizing to the nucleic acid mentioned above or to its complementary nucleic acid under stringent conditions. There is also provided a diagnostic kit for the prognosis of human neuroblastoma containing as the effective ingredient, a primer set comprising a pair of those nucleic acids (DNA).

In addition, this invention provides a method of diagnosing the prognosis of human neuroblastoma, the method comprising detecting the presence or absence of a nucleic acid comprising any one of base sequences set forth in SEQ ID NO:1 to NO:69 in the Sequence Listing from a clinical tissue sample of the neuroblastoma.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a figure corresponding to an electrophoregram showing an example of the results of determination of the gene expression levels in human neuroblastomas with favorable prognosis and with unfavorable prognosis by semi-quantitative PCR.

FIG. 2 is a figure corresponding to electron micrographs showing a primary culture containing SCG neurons of a new born mouse.

BEST MODE FOR CARRYING OUT THE INVENTION

The term “nucleic acid(s)” as used in this invention refers to, for example, DNA or RNA, or polynucleotides derived therefrom which are active as DNA or RNA, and preferably they are DNA or RNA.

The term “hybridize under stringent conditions” means that two nucleic acid fragments hybridize to each other under the hybridization conditions described by Sambrook, J. et al. in “Expression of cloned genes in E. coli”, Molecular Cloning: A Laboratory Manual (1989), Cold Spring Harbor Laboratory Press, New York, USA, 9.47-9.62 and 11.45-11.61.

More specifically, the “stringent conditions” refers to hybridization at approximately 45° C., 6.0×SSC, followed by washing at 50° C., 2.0×SSC. The stringency may be selected by choosing a salt concentration in the washing step from approximately 2.0×SSC, 50° C. as low stringency to approximately 0.2×SSC, 50° C. as high stringency. Also, the temperature in the washing step may be increased from room temperature, or approximately 22° C. as low stringency conditions, to approximately 65° C. as high stringency conditions.

The term “isolated nucleic acid(s)” as used in the present specification refers to a nucleic acid or a polynucleotide containing substantially no cellular substances or culture medium, if prepared by recombinant DNA techniques, or containing substantially no precursor chemical substances or other chemical substances, if prepared by chemical synthesis.

The term “favorable prognosis” as used in the present specification refers to a condition of human neuroblastoma in which the tumor is localized or has become a regressing or benign sympathetic ganglion neoplasm, and is judged to have low malignancy based on N-myc or other tumor markers. According to a preferred embodiment of the invention, a favorable prognosis is a case of stage 1 or 2, with an onset age of less than one year and survival without recurrence for 5 or more years after surgery, and with no noted amplification of N-myc in the clinical tissue; however, there is no limitation to such specific cases. The term “unfavorable prognosis” as used in the present specification refers to a condition of human neuroblastoma in which progression of the tumor has been observed, and it is judged to have high malignancy based on N-myc or other tumor markers. According to a preferred embodiment of the invention, an unfavorable prognosis is a case of stage 4, with an onset age of greater than one year, death within 3 years after surgery and noted amplification of N-myc in the clinical tissue; however, there is no limitation to such specific cases.

The nucleic acids of this invention have been found in the clinical tissues of human neuroblastoma and such nucleic acids have the characteristics described below.

Neuroblastoma is a tumor consisting of actual nerve cells, of which only two types of tumor are known in humans, and analysis of the genes expressed therein is expected to provide very useful knowledge for understanding the biology of nerve cells. Specifically, it is extremely difficult, and practically impossible, to obtain site-specific homogeneous tissue from the brain or peripheral nerves. On the other hand, a neuroblastoma consists of an almost homogeneous nerve cell population (though tumorized) derived from peripheral sympathetic nerve cells, and thus offers a high possibility of obtaining homogeneous expression of neuro-related genes. Furthermore, since neuroblastoma is a type of cancer, it will characteristically have many important genes expressed in the immature stage of neurogenesis.

Clinically and biologically, neuroblastoma can be neatly classified into favorable prognosis and unfavorable prognosis types. Cancer cells from neuroblastoma with favorable prognosis are characterized by having a very slow rate of proliferation, with spontaneous regression beginning at some point. Findings to date have confirmed that nerve cell differentiation and apoptosis (nerve cell death) occur in the spontaneous regression, and that the differentiation which occurs in the maturation stages of normal nerve cells and programmed cell death are phenomena very closely resembling each other. Consequently, it is highly probable that the analysis of genes expressed in such tumors will lead to obtaining important information relating to nerve cell differentiation and apoptosis.

Neuroblastomas with unfavorable prognosis are tumors consisting of cancer cells which continue to exhibit definitely malignant proliferation. The probability is very high, therefore, that they have a large number of important genes connected with nerve cell proliferation or genes expressed in undifferentiated nerve cells. In other words, it is highly probable that these will allow the obtainment of genetic information completely different from the profile of genes expressed in neuroblastomas with favorable prognosis.

It is commonly reported that nerve cells contain more expressed gene types than cells derived from other organs. Neuroblastoma cell lines are derived from clinical tissues with unfavorable prognosis, and it is believed that the gene expression profile in the case of tumor development and progression is substantially altered from that of normal nerve cells.

Neuroblastoma is characteristically a pediatric tumor, and because of the very low possibility of effects by acquired factors, it is expected that analysis of the mechanism of cancerization will also yield embryological information with high probability. More surprisingly, the genes or the gene fragments according to this invention include genes whose expression is enhanced only in specific cell cycle phases, and this further suggests the very strong possibility of obtaining genetic information highly useful for the analysis of cancerization mechanisms and related to development and differentiation.

The nucleic acids, having the characteristics mentioned above and from which the aforementioned information can be obtained, are available from human neuroblastoma clinical tissues and have any of the base sequences set forth in SEQ ID NO:1 to NO:69 in the Sequence Listing, or a portion thereof.

As a result of comparing gene expression levels in clinical tissues from human neuroblastomas with favorable prognosis and with unfavorable prognosis, a highly significant difference was found in each of the nucleic acids having base sequences set forth in SEQ ID NO:1 to NO:69 in the Sequence Listing. That is, the expression of these nucleic acids was enhanced in human neuroblastomas with unfavorable prognosis. Thus, in addition to providing the useful genetic information described above, the base sequences set forth in SEQ ID NO:1 to NO:69 can also be utilized as data for tumor markers to diagnose favorable or unfavorable prognosis of neuroblastoma, by detecting DNA and/or RNA having any of these base sequences.

Specifically, this invention will make it possible to obtain various forms of diagnosis for prognosis on or relating to human neuroblastoma through the following means.

(1) Probes for Hybridization

The nucleic acid comprising a portion or the whole of a base sequence disclosed in this invention (which may be referred to as “nucleic acid(s) of the invention”) may be at least used as a probe for hybridization in order to detect genes expressed in human neuroblastoma. The nucleic acids of the invention can also be used as probes for hybridization in order to determine gene expression in various tumors and normal tissues, to identify the distribution of the gene expression.

When the nucleic acid comprising a portion or the whole of a base sequence disclosed in this invention is used as a probe for hybridization, there are no particular limitations on the actual method of hybridization. As preferred methods there may be mentioned, for example, Northern hybridization, Southern hybridization, colony hybridization, dot hybridization, fluorescence in situ hybridization (FISH), in situ hybridization (ISH), DNA chip methods, and microarray methods.

As one application example of the hybridization, the nucleic acid of this invention can be used as a probe for Northern hybridization to measure the length of mRNA or to quantitatively detect gene expression in an assayed sample.

When the nucleic acid of the invention is used as a probe for Southern hybridization, it enables the detection of the presence or absence of the base sequence in genomic DNA of an assayed sample.

The nucleic acid comprising a portion or the whole of a base sequence disclosed in this invention can also be used as a probe for fluorescence in situ hybridization (FISH) to identify the location of the gene on a chromosome.

The nucleic acid of the invention can also be used as a probe for in situ hybridization (ISH) to identify the tissue distribution of gene expression.

When the nucleic acid of the invention is used as a probe for hybridization, a nucleic acid residue length of at least 40 is necessary; and among the gene sequences according to the invention, a nucleic acid having 40 or more contiguous residues is preferably used. More preferably, one having 60 or more nucleic acid residues is used.

Nucleic acid probe techniques are well known to one skilled in the art, and for example, conditions suitable for hybridization between a probe of specific length according to the invention and the target polynucleotide may be readily determined. In order to obtain hybridization conditions optimal to probes of various lengths, Sambrook et al. “Molecular Cloning: A Laboratory Manual, 2nd Edition, Cold Spring Harbor (1989) may be followed for such manipulations which are well known to one skilled in the art.

The probe of the invention is preferably labeled in an easily detectable fashion. The detectable label may be any type or portion which can be detected either visually or using devices. As commonly used detectable labels there may be mentioned radioactive isotopes such as ³²P, ¹⁴C, ¹²⁵I, ³H and ³⁵S. Biotin-labeled nucleotides may be incorporated into DNA or RNA by nick translation, chemical or enzymatic means. The biotin-labeled probes are detected after hybridization using labeling means such as avidin/streptavidin, fluorescent labels, enzymes, gold colloidal complexes or the like. The nucleic acid may also be labeled by binding with a protein. Nucleic acid cross-linked to a radioactive or fluorescent histone single-stranded DNA binding protein may also be used.

(2) Primers for Use in PCR

For other possible methods of detecting genes, DNA that is the nucleic acid comprising a portion or the whole of a base sequence disclosed in this invention can be used as a primer in a polymerase chain reaction (PCR). For example, RNA may be extracted from a sample to be assayed, and the gene expression can be semi-quantitatively measured by RT-PCR. This may be carried out by a method well known to one skilled in the art. For example, “Molecular Cloning: A Laboratory Manual,” (T. Maniatis, Cold Spring Harbor Laboratory Press) or Idenshibyo Nyumon [Introduction to Genetic Diseases] (Takahisa, S.: Nankodo Publishing) may be followed.

When the DNA that is a nucleic acid of the invention is used as a PCR primer, a base length of 10 to 60 is necessary; and among the gene sequences according to the invention, the nucleic acid having 10 to 60 contiguous bases is preferably used. More preferably, one having 15 to 30 bases is used. Generally, a primer sequence with a GC content of 40-60% is preferred. Also, there is preferably no difference in the Tm values of the two primers used for amplification. Preferably there is no annealing at the 3′ ends of the primers and no secondary structure is formed in the primers.

(3) Nucleic Acid Screening

The nucleic acid comprising a portion or the whole of a base sequence disclosed in this invention can also be used to detect the expression distribution of a gene which is expressed in various tissues or cells. This can be accomplished, for example, by using the nucleic acid of the invention as a probe for hybridization or as a primer for PCR.

Expression distribution of a gene can also be detected using a DNA chip, microarray or the like. That is, the nucleic acid of the invention may be directly attached to the chip or array. RNA extracted from cells of a tissue may be labeled there with a fluorescent substance or the like, hybridized, and an analysis can be made of the type of tissue cells with high expression of the gene. The DNA attached to the chip or array may be the reaction product of PCR using the nucleic acid of the invention. U.S. Pat. No. 5,605,662 to Heller et al. describes an example of the method for attaching nucleic acids to a chip or array.

By utilizing the aforementioned technology, it is possible to use as a diagnostic agent, at least one among the nucleic acids comprising portions or the whole of base sequences disclosed in this invention. In recent years, it has becoming clear that the genetic information possessed by individuals governs their susceptibility to a certain disease as well as governs the effectiveness of a particular drug. The DNA chips or microarrays produced using the aforementioned nucleic acids are used to clarify the cause-effect relationship between the disease of a subject and the nucleic acid, which will enable not only the diagnosis of that disease but also the selection of a drug to be administered. Specifically, if the result detected using the DNA chip or microarray is employed as an indicator of selection of a drug to be administered, the expression level of one nucleic acid among the nucleic acids of the invention can be examined but also the expression levels of two or more nucleic acids can be comparatively examined to select the drug to be administered, which will then enable more accurate judgment. As used herein, the disease is not particularly limited insofar as it is that which can be diagnosed by the nucleic acids of this invention. Preferably, the disease is a neurological disease and more preferably, neuroblastoma.

(4) DNA Cloning

The nucleic acid comprising a portion or the whole of a base sequence disclosed in this invention can be at least used for cloning a gene which is expressed in human neuroblastoma. For example, by using the nucleic acid of the invention as a probe for Northern hybridization or Southern hybridization, or as a primer for PCR, cloning of a gene containing the nucleic acid comprising a portion or the whole of a base sequence disclosed in this invention is possible. As the genes capable of being subjected to cloning there may be mentioned genes with differing levels of expression particularly between neuroblastoma with favorable prognosis and neuroblastoma with unfavorable prognosis, genes whose forms of expression differ in other tissues or cancer cells, genes whose expression is cell cycle phase-dependent, genes induced upon neurodifferentiation and genes whose expression is regulated by oncogenes or tumor suppressor genes.

(5) Methods of Diagnosing Tumor Prognosis and Tumor Markers to be Used Therefor

The nucleic acid comprising a portion or the whole of a base sequence disclosed in this invention can be used as a probe for hybridization, or as a primer for PCR to determine the presence or absence of enhancement in the gene expression in sample cells, which enables the identification of prognosis. To determine the presence or absence of enhancement in the gene expression, any method that utilizes nucleic acids (probes) capable of hybridizing to the nucleic acid comprising any given sequence of the base sequence disclosed in this invention is provided for use. Prognosis can be diagnosed as favorable if the amount of nucleic acid hybridizing to the probe is increased in the sample cell. When the nucleic acid is used as a primer for PCR, RNA is extracted from the sample to be assayed and the gene expression can be semi-quantitatively measured by the RT-PCR method.

(6) Antisense Oligonucleotides

According to another embodiment of this invention there are provided antisense oligonucleotides having the base sequences according to the invention. As will be considered in practicing this invention, the antisense oligonucleotides may readily be prepared such that they can bind to RNA corresponding to the base sequence of this invention and can thereby inhibit the synthesis of RNA.

(7) Gene Therapy

According to a further embodiment of this invention, there are provided therapeutic genes to be used in gene therapy. As will be considered in practicing this invention, the gene according to this invention may be transferred into a vector for use in gene transportation, whereby the transgene can be expressed by an arbitrary expression promoter and can be used for the gene therapy of cancers, for example.

1. Vectors

The transferable viral vectors may be prepared from DNA viruses or RNA viruses. They may be any viral vector of an MoMLV vector, a herpes virus vector, an Adenovirus vector, an AAV vector, a HIV vector, a Seidai virus vector and the like. One or more proteins among the constituent protein group of a viral vector are substituted by the constituent proteins of a different species of virus, or alternatively a part of the base sequence constituting genetic information is substituted by the base sequence of a different species of virus to form a viral vector of the pseudo-type which can also be used in this invention. For example, there is mentioned a pseudo-type viral vector wherein the Env protein (an envelop protein of HIV) is substituted by the VSV-G protein (an envelop protein of vesicular stomatitis virus or VSV) (Naldini L., et al., Science 272, 263-267, 1996). Further, virues having a host spectrum other than human is usable as the viral vector insofar as they are efficacious. As for the vectors other than those of viral origin, there may be used complexes of calcium phosphate and nucleic acid, ribosomes, cation-lipid complexes, Seidai virus liposomes, polymer carriers having polycation as the backbone main chain and others. In addition, methods such as electroporation and gene guns may be used as a gene transfer system.

2. Expression Promoters

As for the expression cassettes to be used for the therapeutic gene, any cassettes without any particular limitations may be used insofar as they can cause genes to express in the target cells. One skilled in the art can readily select such expression cassettes. Preferably, they are expression cassettes capable of gene expression in the cells derived from an animal, more preferably, expression cassettes capable of gene expression in the cells derived from a mammal, and most preferably expression cassettes capable of gene expression in the cells derived from a human. The gene promoters that can be used as expression cassettes include: for example, virus-derived promoters from an Adenovirus, a cytomegalovirus, a human immunodeficiency virus, a simian virus 40, a Rous sarcoma virus, a herpes simplex virus, a murine leukemia virus, a sinbis virus, a hepatitis type A virus, a hepatitis type B virus, a hepatitis type C virus, a papilloma virus, a human T cell leukemia virus, an influenza virus, a Japanese encephalitis virus, a JC virus, parbovirus B19, a poliovirus, and the like; mammal-derived promoters such as albumin, SR α, a heat shock protein, and an elongation factor; chimera type promoters such as a CAG promoter; and the promoters whose expression can be induced by tetracyclines, steroids and the like.

EXAMPLES

This invention will now be explained in greater detail by way of the examples and production examples; however, the invention will not be restricted to those example.

Production Example 1 Construction of cDNA Library from Human Neuroblastoma

1. Obtaining Samples

Human neuroblastoma clinical tissue specimens were quasi-aseptically frozen immediately after surgical extraction and then preserved at −80° C.

2. Selecting Samples with Favorable Prognosis

Prognosis of the samples obtained in 1. above was carried out based on the following criteria.

Favorable prognosis:

-   -   Stage 1 or 2     -   Age of onset less than one year     -   Survival for longer than 5 years after surgery without         recurrence     -   No amplification of N-myc

Unfavorable prognosis:

-   -   Stage 4     -   Age of onset older than 4 years     -   Death within 3 years after surgery     -   Amplification of N-myc

Amplification of N-myc in the aforementioned sample types was confirmed in the following manner.

The clinical tissue obtained in 1. above was thinly sliced with a scalpel and then thoroughly homogenized after addition of 5 ml of TEN buffer (50 mM Tris-HCl (pH=8.0)/1 mM EDTA/100 mM NaCl). Upon adding 750 μl of SDS (10%) and 125 μl of proteinase K (20 mg/ml) to the mixture, it was gently stirred and allowed to stand at 50° C. for 8 hours. This was followed by phenol/chloroform treatment and finally ethanol precipitation to obtain purified genomic DNA. A 5 μg portion of the obtained genomic DNA was completely digested with the restriction endonuclease EcoRI (NEB Inc.), and an N-myc probe was used to determine amplification of N-myc by Southern hybridization.

3. Preparation of mRNA from Clinical Tissue of Human Neuroblastoma with Favorable Prognosis

A 2-3 g portion of the clinical tissue sample of human neuroblastoma judged to have favorable prognosis in 2. above was treated using a Total RNA Extraction Kit (QIAGEN Inc.) and the total RNA was extracted. The extracted total RNA was purified using an oligo dT cellulose column (Collaborative Research, Inc.) to obtain a pool of mRNA with a polyA structure.

4. Dephosphorylation of mRNA

A 100-200 μg portion of the mRNA pool prepared in 3. above was dissolved in 67.3 μl of distilled sterile water containing 0.1% diethyl pyrocarbonate (DEPC), and then 20 μl of 5×BAP buffer (Tris-HCl (500 mM, pH=7.0)/mercaptoethanol (50 mM)), 2.7 μl of RNasin (40 unit/μl: Promega Inc.) and 10 μl of BAP (0.25 unit/μl, bacteria-derived alkali phosphatase: Takara Shuzo Co. Ltd.) were added. The mixture was reacted at 37° C. for 1 hour to effect dephosphorylation of the 5′ end of the mRNA. This was followed by phenol/chloroform treatment two times, and finally ethanol precipitation to obtain a purified dephosphorylated mRNA pool.

5. Decapping of Dephosphorylated mRNA

The total amount of the dephosphorylated mRNA pool prepared in 4. above was dissolved in 75.3 μl of distilled sterile water containing 0.1% DEPC, and then 20 μl of 5×TAP buffer (sodium acetate (250 mM, pH=5.5)/mercaptoethanol (50 mM), EDTA (5 mM, pH=8.0)), 2.7 μl of RNasin (40 unit/μl) and 2 μl of TAP (tobacco acid pyrophosphatase: 20 unit/μl) were added. The mixture was reacted at 37° C. for 1 hour to effect decapping treatment of the 5′ end of the dephosphorylated mRNA. The dephosphorylated mRNA of incomplete length with no capped structure remained without decapping, and with the 5′ end dephosphorylated. This was followed by phenol/chloroform treatment and ethanol precipitation to obtain a purified decapped mRNA pool.

6. Preparation of Oligo-Capped mRNA

The total amount of the decapped mRNA pool prepared in 5. above was dissolved in 11 μl of distilled sterile water containing 0.1% DEPC, and then 4 μl of 5′-oligo RNA (5′-AGCAUCGAGUGGGCGUUGGCCUACUGG-3′ (SEQ ID NO: 70): 100 ng/μl), 10 μl of 10× ligation buffer (Tris-HCl (500 mM, pH=7.0)/mercaptoethanol (100 mM)), 10 μl of magnesium chloride (50 mM), 2.5 μl of ATP (24 mM), 2.5 μl of RNasin (40 unit/μl), 10 μl of T4 RNA ligase (25 unit/μl: Takara Shuzo Co. Ltd.) and 50 μl of polyethylene glycol (50% w/v, PEG8000: Sigma Corporation) were added. The mixture was reacted at 20° C. for 3 hours for ligation of the 5′-oligo RNA to the 5′ end of the decapped mRNA. The dephosphorylated mRNA of incomplete length with no capped structure resulted in no ligation to the 5′-oligo RNA. This was followed by phenol/chloroform treatment and ethanol precipitation to obtain a purified oligo-capped mRNA pool.

7. Removal of DNA from Oligo-Capped mRNA

The oligo-capped mRNA pool prepared in 6. above was dissolved in 70.3 μl of distilled sterile water containing 0.1% DEPC, and then 4 μl of Tris-HCl (1 M, pH=7.0), 5.0 μl of DTT (0.1 M), 16 μl of magnesium chloride (50 mM), 2.7 μl of RNasin (40 unit/μl) and 2 μl of DNaseI (5 unit/μl: Takara Shuzo Co. Ltd.) were added. The mixture was reacted at 37° C. for 10 minutes to dissolve the excess DNA. This was followed by phenol/chloroform treatment and ethanol precipitation and column purification (S-400HR: Pharmacia Biotech Inc.), to obtain a purified DNA(−) oligo-capped mRNA pool.

8. Preparation of 1st Strand cDNA

The DNA(−) oligo-capped mRNA pool prepared in 7. above was reverse transcribed using SuperScript II (kit by Life Tech Oriental, Inc.) to obtain a pool of 1st strand cDNA. The pool of DNA(−) oligo-capped mRNA was dissolved in 21 μl of sterile distilled water, and then 10 μl of 10× First Strand buffer (kit accessory), 8 μl of dNTP mix (5 mM, kit accessory), 6 μl of DTT (0.1 M, kit accessory), 2.5 μl of oligo-dT adapter primer (5 pmol/μl, 5′-GCGGCTGAAGACGGCGTATGTGGCCTTTTTTTTTTTTTTTTT-3′ (SEQ ID NO: 71)), 2.0 μl of RNasin (40 unit/μl) and 2 μl of Superscript II RTase (kit accessory) were added. The mixture was reacted at 42° C. for 3 hours to effect reverse transcription. This was followed by phenol/chloroform treatment, alkali treatment and neutralization treatment to dissolve all the RNA and purification was carried out by ethanol precipitation.

9. Preparation of 2nd Strand cDNA

The 1st strand cDNA pool prepared in 8. above was subjected to PCR amplification using Gene Amp (kit by Perkin Elmer Inc.). The pool of 1st strand cDNA was dissolved in 52.4 μl of sterile distilled water, and then 30 μl of 3.3× Reaction buffer (kit accessory), 8 μl of dNTP mix (2.5 mM, kit accessory), 4.4 μl of magnesium acetate (25 mM, kit accessory), 1.6 μl of Primer F (10 pmol/μl, 5′-AGCATCGAGTCGGCCTTGTTG-3′ (SEQ ID NO: 72)), 1.6 μl of Primer R (10 pmol/μl, 5′-GCGCTGAAGACGGCCTATGT-3′ (SEQ ID NO: 73)) and 2 μl of rTth (kit accessory) were added. A 100 μl portion of mineral oil was gently added to the mixture and overlayed thereon. After denaturing the reaction solution at 94° C. for 5 minutes, a cycle of 94° C. for 1 minute, 52° C. for 1 minute and 72° C. for 10 minutes was repeated 12 times, and then the solution was allowed to stand at 72° C. for 10 minutes to complete the PCR reaction. This was followed by phenol/chloroform treatment and ethanol precipitation to obtain a 2nd strand cDNA pool.

10. SfiI Treatment of 2nd Strand cDNA

The 2nd strand cDNA pool prepared in 9. above was dissolved in 87 μl of sterile distilled water, and then 10×NEB buffer (NEB Inc.), 100×BSA (bovine serum albumin available from NEB Inc.) and 2 μl of SfiI (restriction endonuclease, 20 unit/μl, NEB Inc.) were added. The mixture was reacted overnight at 50° C. to effect SfiI restriction endonuclease treatment. This was followed by phenol/chloroform treatment and ethanol precipitation to obtain a pool of cDNA which had been SfiI-treated at both ends.

11. Size Fractionation of SfiI-treated cDNA

The SfiI-treated cDNA pool prepared in 10. above was electrophoresed on 1% agarose gel and a fraction with >2 kb was purified using Geneclean II (Bio101 Inc.). The purified cDNA pool was dissolved in 100 μl of sterile distilled water and allowed to stand at 37° C. for 6 hours. This was followed by phenol/chloroform treatment and ethanol precipitation to obtain a long-chain cDNA pool.

12. Preparation of cDNA Library

The long-chain cDNA pool prepared in 11. above was ligated into the cloning vector pME18S-FL3 (provided by Prof. Sumio Kanno of the Institute of Medical Science, Tokyo University) using a DNA Ligation Kit ver.1 (kit by Takara Shuzo Co. Ltd.). The long-chain cDNA pool was dissolved in 8 μl of sterile distilled water, and then 1 μl of pME18S-FL3 pretreated with restriction endonuclease DraIII, 80 μl of Solution A (kit accessory) and 10 μl of Solution B (kit accessory) were added and reaction was conducted at 16° C. for 3 hours. This was followed by phenol/chloroform treatment and ethanol precipitation for purification to obtain a cDNA library.

Example 1 Transformation into E. coli

The cDNA library prepared in Production Example 1 above was used for transformation into E. coli (TOP-10: Invitrogen Corporation). The cDNA library was dissolved in 10 μl of sterile distilled water and mixed with TOP-10. The mixture was then incubated on ice for 30 minutes, at 40° C. for 1 minute and on ice for 5 minutes. After adding 500 μl of SOB medium, shake culturing was performed at 37° C. for 60 minutes. Appropriate amounts thereof were seeded onto ampicillin-containing agar media and culturing was continued at 37° C. for a day and a night to obtain E. coli clones.

The E. coli clones on agar media obtained were collected with toothpick and suspended in 120 μl of LB medium prepared in a 96-well plate. The 96-well plate was then allowed to stand overnight at 37° C. for culturing of the E. coli. A 72 μl portion of 60% glycerol solution was then added and preserved at −20° C. (glycerol stock).

Example 2 Base Sequence Determination

1. Preparation of Plasmid

The 10 μl of glycerol stock prepared in Example 1 was transferred to a 15 ml centrifugation tube, and then 3 ml of LB medium and 50 μg/ml of ampicillin were added and shaking was carried out overnight at 37° C. for culturing of the E. coli. A QIAprep Spin Miniprep Kit (QIAGEN Inc.) was then used to extract and purify a plasmid DNA from the E. coli.

2. Analysis of Both End Sequences

Both end sequences of the plasmid DNA prepared in 1. above were determined using a DNA Sequencing Kit (kit by ABI). There were combined 600 ng of plasmid DNA, 8 μl of premix (kit accessory) and 3.2 pmol of primers, and sterile distilled water was added to a total of 20 μl. After denaturing the mixture at 96° C. for 2 minutes, a cycle of 96° C. for 10 seconds, 50° C. for 5 seconds and 60° C. for 4 minutes was repeated 25 times for reaction. The product was then purified by ethanol precipitation. Sequencing was carried out by polyacrylamide gel electrophoresis under denaturing conditions, using ABI377 (ABI).

Example 3 Homology Search Using Database

An Internet-mediated DNA sequence homology search was conducted for the samples on which the both end-sequences were analyzed in Example 2. The homology search was conducted using the BLAST of the NCBI (National Center of Biotechnology Information, USA).

Example 4 Determination of Gene Expression Levels in Human Neuroblastomas with Favorable Prognosis and Unfavorable Prognosis by Semi-Quantitative PCR

PCR primers were synthesized from portions of the genes obtained in Example 3, and the expression levels in the clinical tissues of human neuroblastomas with favorable prognosis and unfavorable prognosis were comparatively quantitated. mRNA was extracted from the human neuroblastoma clinical tissues by the method described in Example 1, and rTaq (Takara Shuzo Co. Ltd.) was used for PCR reaction. Specifically, 5 μl of sterile distilled water, 2 μl of mRNA, 1 μl of 10×rTaq buffer, 1 μl of 2 mM dNTPs, 0.5 μl each of the synthesized primer set and 0.5 μl of rTaq were combined. After denaturing the mixture at 95° C. for 2 minutes, a cycle of 95° C. for 15 seconds, 55° C. for 15 seconds and 72° C. for 20 seconds was repeated 35 times, and then the mixture was allowed to stand at 72° C. for 6 minutes for PCR reaction. The reaction solution was subjected to 1% agarose gel electrophoresis. One example of the results of determination of the gene expression levels in human neuroblastomas with favorable prognosis and unfavorable prognosis by semi-quantitative PCR is shown in FIG. 1. Here, the explanations of the respective lanes are as follows:

-   Lanes 1-8: expression of the gene corresponding to the nucleic acid     comprising the base sequence set forth in SEQ ID NO: 21 in the     Sequence Listing in a clinical sample of neuroblastoma with     favorable prognosis; -   Lanes 9-16: expression of the gene corresponding to the nucleic acid     comprising the base sequence set forth in SEQ ID NO: 21 in the     Sequence Listing in a clinical sample of neuroblastoma with     unfavorable prognosis; -   Lanes 17-24: expression of GAPDH in a clinical sample of     neuroblastoma with favorable prognosis; and -   Lanes 25-32: expression of GAPDH in a clinical sample of     neuroblastoma with unfavorable prognosis.

Consequently, nucleic acids whose expression is enhanced only in human neuroblastoma with unfavorable prognosis have been identified in the base sequences set forth in SEQ ID NO:1 to SEQ ID NO:69.

Example 5 Gene Group with Varying Gene Expression Levels by NGF Regulated Apoptosis in Murine Superior Cervical Gangliocytes.

It is known that NGF (nerve growth factor) exerts protective action against apoptosis in human neuroblastoma induced by an antimitotic agent (such as neocarzinostatin). (Cortazzo M H, J. Neurosci, 16, 3895-3899 (1996)). This action is believed to be due to the inhibition of apoptosis by the binding of NGF to p75. It has also been pointed out that the regression of neuroblastoma (causing favorable prognosis) at clinical stage is connected to the apoptosis of the tumor cells.

In order to identify the apoptosis-associated genes in neuroblastoma, the gene group with varying gene expression levels by NGF regulated apoptosis in murine superior cervical gangliocytes was examined.

Superior cervical gangliocytes (SCG neurons) were first isolated from C57BL/6J mice (0 to 1 day of age) in 7 to 10 animals. Seven wells of cells were arranged to be grown on a 24-well cell culture plate at about 1 to about 2×10⁴ cells per well. RNA was further collected from about 1 to about 2×10⁴ cells (Day 1 as control).

After the culture obtained by adding NGF (5 mg/ml) to the 7-well cells was incubated for 5 days, RNA was collected from one-well cells (+NGF; after 5 days). Cultures in three wells each of the 6 wells were exchanged with cultures with addition of NGF (5 mg/ml) or anti-NGF antibodies (1%), and they were respectively incubated for 12 hours, 24 hours and 48 hours. Using portions of the samples, cells were examined under an electron microscope to identify the morphological differences between the case where NGF had been added and the case where anti-NGF antibodies had been added. The results are shown in FIG. 2. NGF induced differentiation was observed in the cells with NGF addition, whereas apoptosis was observed in the cells with anti-NGF antibody addition. As a result of NGF depletion by the anti-NGF antibodies, it was apparent that apoptosis was induced. RNA was collected from the respective well cells after 12 hr, 24 hr, and 48 hr culturing. These samples were denoted +NGF 12 hrs, +NGF 24 hrs, +NGF 48 hrs, −NGF 12 hrs, −NGF 24 hrs, and −NGF 48 hrs.

As described above, RNAs of the respectively treated cells from approximately 160 mice were concentrated by ethanol precipitation and cDNAs were synthesized from 1 g RNAs using reverse transcriptase. These cDNAs were used as templates and gene expression levels were compared by PCR. The primers used were constructed from the homologous genes in mice based on the genes found in human neuroblastoma cells. The base sequences of the primers used for the comparison of expression are summarized in Table 1 together with the gene identification numbers (ID) for the targeted genes for comparison.

TABLE 1 SEQ SEQ primer ID NO primer sequence primer ID NO primer sequence nbla00031m-F3 74 TCAGAAGGCTTCGAGACTG nbla00031m-R3 75 GCAGATATCTTGTCAAAGGT nbla00100m-f 76 GGTGAGCCCTAACATCCACA nbla00100m-r 77 AGCCCGTAAGCCATCAATC nbla00115m-F3 78 ATCATGGTGAAAGGCACGTC nbla00115m-R3 79 CATAATTTCCACGTGTTGTG nbla00116m-F3 80 AGAGGTTAGCCCTGAGACAG nbla00116m-R3 81 TCTATGCTTCCAGCAGGTAC nbla00124m-F3 82 CCTTTATATTAGAACGTGGC nbla00124m-R3 83 TAGGTTTTCAGGACTTGG nbla00144m-F 84 GCAGGATAGCAACCTTGACA nbla00144m-R 85 ATGCATGCTTTCGTGTGTTC nbla00150m-2f 86 CACCCTGGAGAAACACAAACTC nbla00150m-2r 87 ATGCCGTCCATCTTCATCAC nbla00170m-F3 88 AACATGAATCTGTGGGTGAC nbla00170m-R3 89 TCAATCGCTTGACCTTTCCTC nbla00204m-F3 90 AAGCATTGAAGTAACAACCG nbla00204m-R3 91 TGCATTTGACATATGAGAGC nbla00225m-F2 92 TATTAGAACGTGGCCCTCCA nbla00225m-R2 93 TCGGGACTAGCAGGACAGAA nbla00301m-F3 94 TAAACCAGCAACCCTAACAG nbla00301m-R3 95 ACTAGAATCAGACCTGCCTT nbla00315m-F 96 AACTGGCAGCAAAGAAGGTC nbla00315m-R 97 AGCAGAAGCACGTCAGTAAGG nbla00402m-F2 98 TCACCCAGAATGAGACATGG nbla00402m-R2 99 GTCAGAAGGTGACACGGTGA nbla00433m-F3 100 CCCAAGGAGGTAAGAGCCTG nbla00433m-R3 101 AAGCGCTGGAGCTTGTCGGT nbla00437m-F3 102 AGAACGGTGTAATTCAGAGA nbla00437m-R3 103 GTCATCAGCAAGCTCGAATA nbla00537m-F3 104 TTTATATTAGAACGTGGCCC nbla00537m-R3 105 AGGACTTGGTAGCTTCTCGG nbla00551m-F 106 AATTTTAAAAAGGCAGGATATACAAC nbla00551m-R 107 AAGGAGAGGTAGCATTTTATGTGC ori00660m-F 108 GGCATCCTCATCTCCTCAGA ori00660m-R 109 TCTGAAGCAGTTCGAAGCAC nbla00761m-f 110 TGGTTCAAACTCTTCCCTCCT nbla00761m-r 111 CTTCCACCTGTGCGTTTTCT nbla00831m-F3 112 TGGGAAATCCACCTGCATC nbla00831m-R3 113 ACCAGCTCACCCTGAATGTG nbla00908m-2f 114 CGTGGCAACACCTTTTTATTC nbla00908m-2r 115 ACACGGCATGGGTTTGTT nbla02874m-f 116 TGAGGAGTTGAATGCTGACCT nbla02874m-r 117 CATCGGGGTTAATGCTCTTG nbla03086m-f 118 ACTTGCTCATGGTGCTGTCTC nbla03086m-r 119 CGCAGAGCCTGGTAATCTTC nbla03113m-F 120 CCTCAAGAACCAGACCAAGC nbla03113m-R 121 CTGATGCTGAGGAGCTGACA nbla03199m-f 122 GGCCACCAGAGAGGTAATG nbla03199m-r 123 GTGCTGACCTAAGACCCAAAG nbla03267m-f 124 CTGCCTTTGAGATGGTGATG nbla03267m-r 125 TGTAGTGCTTTGCATTGTTGG nbla03646m-f 126 TACCTCTTCGGCTGGATGG nbla03646m-r 127 GCTTGGGCAGGATGAATG nbla03755m-F 128 AGCCGATGAAGTGTCTGCTT nbla03755m-R 129 RAGCCACAAAAGCAGGTTAGG nbla03771m-f 130 GCAGCAGATATAGGGACACAGA nbla03771m-r 131 CACGCATAAATGGCTACACC nbla03777m-F3 132 AGATTATTCACCTGTAAGC nbla03777m-R3 133 TTTTCCACATGTCCAGCACC nbla03831m-f 134 GTGACCAGCAAGGAAACACA nbla03831m-r 135 GAGGATTCAGCCACGAACA nbla03862m-F 136 GCATGGAGGAAACCATTAGG nbla03862m-R 137 TGGCTCTTCAACCAAACCTT nbla04021m-F2 138 ATGACCTGGCACTAGGCTTG nbla04021m-R2 139 AACACATCTGCTGGCTTCTG nbla04137m-f 140 ACGACGACACTGACAACCAC nbla04137m-r 141 GCTTGACCTCCGACTCATCT nbla04196m-f 142 CACCCATCTGTGTCTGTGGT nbla04196m-r 143 CGTGCTGACGATGATGTTG nbla04261m-2f 144 GTGTTTGGCACTACATCACCA nbla04261m-2r 145 CCGGGTTTTCCATTTTCAC nbla04300m-f 146 TACAGTGGGAACTGCGTTTG nbla04300m-r 147 CAGGGTTCGTATGCAGGAG nbla10058m-f 148 AGCCATTACAGGTGGCAAGA nbla10058m-r 149 GTTGGGTCGATCTTAGGAGGTAG nbla10070m-F3 150 TAACAACTCTAGCACCATC nbla10070m-R3 151 TACTTAGCAGAACAGAAGAG nbla10071m-f 152 GTGGACACCAAGAATGCAAG nbla10071m-r 153 CAGCCAACTGTGGTAAGAAGG nbla10120m-F 154 CAGTGCAGCCTTGGAAGTGT nbla10120m-R 155 TCAAAAGCTGCGTGTGTCTC nbla10143m-F3 156 TTAGTGAGTACACGAGCTGG nbla10143m-R3 157 ACTTAACCCAGACTGACCAC nbla10283m-F3 158 AGATGTTTAAGGGCAAACC nbla10283m-R3 159 TGGAGCCTCTTGGATCTC nbla10300m-F3 160 AACATCCTGGTGGAACAGC nbla10300m-R3 161 CTCTATAGTAACGACCAAAC nbla10314m-f 162 GCTTGAGGACAGTGAAAACCA nbla10314m-r 163 TGGAGTGAGAGGATGGGAAG nbla10317m-2f 164 GCAGGGGACACAGGACTCTAC nbla10317m-2r 165 AAGCTCCTTCTGGCTCAACA nbla10329m-F 166 CCGAGATCTTCTGCCTTCAT nbla10329m-R 167 TCCTTGCCGTCTCAAACTCT nbla10363m-F3 168 ATCTCTCTAGTGCCATGAC nbla10363m-R3 169 AGTCTTGCTAAGACTTTCAG nbla10383m-f 170 CAGTGCGGTTGTGGTCTATCT nbla10383m-r 171 TGAGGCGTTGACTTTCTGG nbla10388m-F 172 TTCAGCAGGTCCTAGCCAAG nbla10388m-R 173 RTGGAAGCTGCTGAAGAAACA nbla10457m-F 174 GCCTTTCTTTGTCTGGAACG nbla10457m-R 175 GGGTGAAGCAATTTCACAGG nbla10485m-F 176 AAATGGCAGTTTGACTGTGG nbla10485m-R 177 TTGGCTGAGTTCTCCCTCAT nbla10527m-F3 178 ATTAATCCTGCACTCTTACG nbla10527m-R3 179 AGTTCCATTTCTACAGCAAG nbla10535m-F 180 TTGGTCGTGAGGTGGATTCT nbla10535m-R 181 ATCTTGCCAGCCACAGACTT nbla10545m-F 182 AGAGTCACCTGCGACCCTTA nbla10545m-R 183 AGCTCTAGCAGCCAGCACAT nbla10677m-f 184 CATAATCTTCTCCGGCTTCATC nbla10677m-r 185 GTCTGGTATTTCCGTGAGGTTT nbla1087m-F3 186 ATCTCCCATCGACTCACTGC nbla10687m-R3 187 TGGCTTTACTGGTCATACAG nbla10696m-f 188 TGATTCTCCAAGGCAAGGT nbla10696m-r 189 GATTTCCCCATTGACTGCT nbla10988m-2f 190 AGCCTTTGCTACCCTCTTCC nbla10988m-2r 191 GGCGAAACACTCCTCTCGT nbla11030m-F3 192 AACCTCGTAAAAACCATGGC nbla11030m-R3 193 AGCAGTGACTTGAGCATTTG nbla11042m-2f 194 CGACACCTCTCATTGCACAC nbla11042m-2r 195 TCCGTCTCAAATCCACACAC nbla11051m-f 196 AGCACAATTCCCCAGACAC nbla11051m-r 197 CTGTAGCCCTTACTGTTTGACC nbla11189m-F 198 CTGTGTTCTGATGCCAATGC nbla11189m-R 199 TGCAACTTTCTCCACCAAGA nbla11589m-F2 200 GGAGCTAGCCAAGATGATCG nbla11589m-R2 201 CTGGCCATCCTAGAGGAGAA nbla11882m-F 202 AATTTTAAAAAGGCAGGATATACAAC nbla11882m-R 203 AAGGAGAGGTAGCATTTTATGTGC nbla11895m-F3 204 AATCTTCCTCCCAACCCATG nbla11895m-R3 205 TGACCCTGCTGAAGGAAGCG nbla20001m-F2 206 CCCTGAATGTTGAACGAGTG nbla20001m-R2 207 TGCACATTGAAGAGGCAAAC nbla20019m-F1 208 CCGAGGTCAACATTTGTTCC nbla20019m-R1 209 GAGCAGAGCACAGACAGTGG nbla20125m-F1 210 CTGGAATCATCCAGGCTTTG nbla20125m-R1 211 GCGTCCAGGATAACAGCACT nbla20134m-F1 212 GTCTTCAAGCAGCGACAGTG nbla20134m-R1 213 CCTTCAGGGTCTGGTTGATG nbla20146m-F1 214 GGGACCACTAACCAGCTGAA nbla20146m-R1 215 AAATGTCTGACCCCTCCTCA nbla20181m-F1 216 CCAGGATGGAGTAGCCAAGA nbla20181m-R1 217 GCCAGTGATCTCCAGGTTTG nbla20182m-F1 218 ACTGGGGAGGAATGGCTAGT nbla20182m-R1 219 CTGGCTGGAGGAAAAAGGAC nbla20211m-F1 220 CTGAGGTGCTGATGATCCTG nbla20211m-R1 221 CCAAACTCCTGCTCTTCTCG nbla20231m-F1 222 AGCAGTTTGGTGCTGTTGGT nbla20231m-R1 223 GCTTGTTCCATGGTTGGACT nbla20250m-F2 224 ACGAGGACCACAGGACTCAA nbla20250m-R2 225 TGGGCTCCATAGTTTGTTCC nbla20268m-F1 226 ATTCTCTCTGGAGGCGATGA nbla20268m-R1 227 TTTCCTCACAGCTCCCTCTC nbla20378m-F2 228 TTTAGCTGTTTGCAAATAAGATGT nbla20378m-R2 229 AATGCAGTGTGTGGGATGTG nbla20421m-F1 230 TCCGACATGATGGTTCTCCT nbla20421m-R1 231 AGATCCAGGAGTCACCCAAA nbla20487m-F3 232 CACAGGTGTCAAAGCACGTT nbla20487m-R3 233 TGTAGCACTCGCTGTTGCTC nbla20511m-F1 234 TCCTGAAGCCTTCTTGCCTA nbla20511m-R1 235 GCTTGTGGCAACCAGAAAGT nbla20541m-F1 236 AGGTGGGAGTCGACCTTTCT nbla20541m-R1 237 GCATCCTTCAACTTGGTCCT nbla20638m-F1 238 GCAGCAAGGAAGAGGACAAG nbla20638m-R1 239 AGCAATCTTCGTCTGGGAAG nbla20688m-F1 240 AGAAGGACCTCCTCCCAAAG nbla20688m-R1 241 TGCAACAGTCCTCTTCCTTG nbla20709m-F2 242 ATTAGTTGGGACCTGCCTTG nbla20709m-R2 243 GCCCATTTTCTTCAGCAGAG nbla20765m-F1 244 AGAGCAGCTCAGCTACCACA nbla20765m-R1 245 GAAGGCAACTTTGGTGTTGG nbla20798m-F1 246 AAACGGGTACAGGATGGAGA nbla20798m-R1 247 CAACTGGAGGTCGGAGGATA nbla20874m-F1 248 TGGTCTGTTTAACAATTGACCTG nbla20874m-R1 249 GCTGCATCTTCCAACATTCTT nbla20968m-F1 250 CCGTGCAGTTTGACATGAAT nbla20968m-R1 251 TGTGGCATCTCATTCAGCAT nbla21013m-F1 252 CACCCTTTGAAGTGACGGTA nbla21013m-R1 253 CTGAAAAACCAGCCCACACT nbla21024m-F1 254 CTCTGTGGGATGACACATGC nbla21024m-R1 255 TTTGGCACCTTGTCATTTTG nbla21077fm-F1 256 CCTGCTTAAGAGTAAGCCTGGT nbla21077fm-R1 257 AGTTCTGTGGGCTATAGGATCG nbla21130m-F1 258 TGTGTCTTCCGACTTTCTGG nbla21130m-R1 259 TCTTTCCCTGAGTGCTTGGT nbla21189m-F1 260 AGAGGTGGAAGCACTTCAGG nbla21189m-R1 261 AAAGTCCTTGGTGCTCTCGT nbla21233m-F1 262 CTGGAGCCTGTTTGATGGTT nbla21233m-R1 263 TGCTTTCCTTACTGGCAGGT nbla21266m-F1 264 GAACATGGGCACTGACTGG nbla21266m-R1 265 CATCAGGGCTAGGAGACTCG nbla21297m-F3 266 CAGCAATGAATCCTCCAATGT nbla21297m-R3 267 TGGTGGTTCTCCCTGTGATT nbla21298m-F2 268 AGACCAGTGGCTCGTCAAAC nbla21298m-R2 269 TTGCAGACATCAGGGGTGT nbla21337m-F2 270 TCTGCACCAGAGAATCCACA nbla21337m-R2 271 ATAGGGCTTTTCTCCCGTGT nbla21367m-F1 272 CAGAAAAACGGTGGAGGACT nbla21367m-R1 273 CCCTGCCTTGTTCTCCATAA nbla21375m-F1 274 CAAGCATGCAGGAAGAACTC nbla21375m-R1 275 AATGTTCGTAGCCGATCCAG nbla21413m-F1 276 TGTGTTTGCTGGGGAGTATG nbla21413m-R1 277 TCATTTGCAGCCACTCTACG nbla21569m-F1 278 TGGAGCTCAGAAGAGGAGGA nbla21569m-R1 279 CGCAACATGAAGTCCATCAG nbla21681m-F1 280 CAAAGTCCCTCTCCTTCAGC nbla21681m-R1 281 CCCTAGTGGCCAACTCTGAT nbla21761m-F1 282 TTACCCAGGTGGTTCAGCAT nbla21761m-R1 283 TACCCATCAGGGTGATGACA nbla21843m-F1 284 GCCAGGAAGTGAGGAATGAG nbla21843m-R1 285 CCCGGATGACCTGAATGTAG nbla21855m-F1 286 AACACACTGGCGTTCATCTG nbla21855m-R1 287 GACTCCCACTTGCGTCTCTG nbla21922m-F1 288 GACATGGAAGGCATGCTGTA nbla21922m-R1 289 GACAGACGCTTCAGCGAAAT nbla21934m-F1 290 AGCCTTGGTGCTGAAGATGT nbla21934m-R1 291 CTTATGTGACCGTGCACCTG nbla21936m-F1 292 CGCCTGACAATCTCAATTCC nbla21936m-R1 293 CTCACGTGTCTGCGTTTGAT nbla21950m-F1 294 AGGGGATCCGGAAGTATGAC nbla21950m-R1 295 AAGCCGCTCATCTGGTAGAG nbla22027m-F1 296 TGAGAAAACGGTCCTGAAGC nbla22027m-R1 297 TGTCAGACCCTTGGCATCTT nbla22028m-F1 298 TACCTGAGTCGGACACGATG nbla22028m-R1 299 GAGAGCCAGACAAGCTTTGG nbla22093m-F1 300 ACAAGGACCCCTGTGCTAAC nbla22093m-R1 301 TGAGGACAGTGGCAGGTGTA nbla22153m-F1 302 TGCGAGGATTAACTCCAAGG nbla22153m-R1 303 GGCAACTTTGGCTGAAGAGT nbla22182m-F2 304 AGTCCCCATTGGGATACTGC nbla22182m-R2 305 TGGGCAATAATTTGGAAACC nbla22218m-F1 306 AGCCACACTGTTAGCAGCAA nbla22218m-R1 307 CGAATGTCCAGAAGGGAGAG nbla22228m-F1 308 CAGCCTGTGAATGGTGTGAA nbla22228m-R1 309 TGAGGGAAGCTGTGGAAGAG nbla22298m-F1 310 TGACATCTGCTTGTCCTTGG nbla22298m-R1 311 GGACGGCAGTACCAAGAGTG nbla22344m-F2 312 GAGTCTGCCATTGGCTTTGT nbla22344m-R2 313 CTGCTTGCTCTGTTCCACTG nbla22351m-F1 314 AGACAGGGTCTGGCTGTGTT nbla22351m-R1 315 TGAGGCCAGGAGTTCAAGAC nbla22352m-F1 316 CTGGCACAATGTCTTCACAA nbla22352m-R1 317 TTGAAAGGGGAGATTCCTGA nbla22361m-F1 318 CGACAGATGACCTTGATTCG nbla22361m-R1 319 GCCTCAGAAGCCTTTCTCAA nbla22382m-F1 320 GTTGGCGAGCTAGCAAAACT nbla22382m-R1 321 TGCCATCCTTCTCACAGATG nbla22394m-F1 322 TTACCCATAATGCCCTCCAC nbla22394m-R1 323 CAAAACGACAGCAGCAGAAC nbla22451m-F1 324 GGCATTGGAGGTTGTCATTC nbla22451m-R1 325 GCTTGCTCTTCACCAGGAAC nbla22455m-F1 326 GAAGACCCTGGTTTTTGCAG nbla22455m-R1 327 CAACTCGGTTGGTGAAATCAG nbla22465m-F1 328 AGGAGAAGCCTCATCAACCA nbla22465m-R1 329 TCAGGCAGACATTCCCAGAT nbla22474m-F1 330 AATGTGCCGGTTTTCTCATC nbla22474m-R1 331 CCAACCCCTTAGACATGCAC nbla22549m-F1 332 TCTGTGAAAGGGCATGTGAG nbla22549m-R1 333 GGAGGGATTTCATTGCTCTG nbla22704m-F1 334 TCTCAGTTGGGTTTGGAAGC nbla22704m-R1 335 GGAGAAAAGCCAGAGTGTCG nbla22832m-F1 336 CACGGGAACCCATTTGTATG nbla22832m-R1 337 GTGGAAGGAGCCGTTGATAA nbla22886m-F1 338 ATCGGCAGAGTGCATACCTT nbla22886m-R1 339 TCTGTGGCTCAATACGCTTG nbla23020m-F1 340 TTCCCACCAAATCAGTCTCC nbla23020m-R1 341 TGGCCACTGAAGTCTCAGGT nbla23028m-F1 342 ATGGTGAAAGTGGTTCAGTGC nbla23038m-R1 343 TGCATTTGCTGTGGATTACC nbla23060m-F1 344 GTGGCACAGTGGGAGCTATT nbla23060m-R1 345 GCCCAATCCTCTAAACAACG nbla23218m-F1 346 GTAAACAGCCCCTTGGTCAG nbla23218m-R1 347 ATGTGCAGTGTTCCCCACTT nbla23394m-F1 348 CAAGCGGTGGAGTACTTGAA nbla23394m-R1 349 CCTGCAGTTCCCAGTCTTTC nbla23512m-F1 350 CCCAGCCAGCCAAGTAGATA nbla23512m-R1 351 ACCCCACTCTTTGGGTCTCT nbla23653m-F1 352 ACTGGGCATCTGGATAGCAG nbla23653m-R1 353 CTTCGGAACCAGCCAACTTA nbla23664m-F1 354 TGAGGGGCTTCAAGCAGTAG nbla23664m-R1 355 GCACACTCACTTCCCAAGGA nbla23666m-F1 356 CGTGGTGGTGTGTATTTTGG nbla23666m-R1 357 GCGGTGACATAAAAGGCTGA nbla23718m-F1 358 ATGGAGAACTTGCCTGCACT nbla23718m-R1 359 TCAGCTTCACCCACACTTTG nbla23719m-F1 360 CTGTGGAGGAGTGGGATGTT nbla23719m-R1 361 GTTGCTTTTGGTTTCCCATC nbla23760m-F1 362 TGTGAGTCCTCCTGTTGTGG nbla23760m-R1 363 GAGCTGTCAAAATGGCTTCC nbla23951m-F1 364 TCACAGTTGCTGCCAAAGAG nbla23951m-R1 365 CGTCCCATTTTCCAGAGATG nbla23973m-F1 366 ACCAGTGTGAGGTGGTCAGA nbla23973m-R1 367 GTGGGAGGCCACAAACTTAG nbla24082m-F1 368 GGAGCAATCCAAGGAGATGA nbla24082m-R1 369 TGGACAGCCTCCTTCAGTTT nbla24084m-F1 370 GGTCGTTTAGGTGGCAAATG nbla24084m-R1 371 CCCAGGAATCTGCAAGGATA nbla24104m-F1 372 GTTGATGGAGCACCACAGAA nbla24104m-R1 373 CTGCATTGTTCAGCCAGGTT nbla24131m-F1 374 CACCAATGCTGTGAACTTGC nbla24131m-R1 375 TGACAGTCCAGCCTCACAGA nbla24239m-F1 376 TGGACACGCATAAGAAGCAG nbla24239m-R1 377 TGTCGAAGAAACTCCTGACG nbla24285m-F1 378 GTGGTGTGATGTCTGCCATT nbla24285m-R1 379 CCTTGTTGGACCTTGATTCC nbla24297m-F1 380 AAGGCTCTTTCCAGGAGGTC nbla24297m-R1 381 CCTTCAGGACACACAGGCTTA nbla24348m-F1 382 TAGTCCCCAAACCTGCTGTT nbla24348m-R1 383 GGCGAAGAAGAATTTGAACG nbla24434m-F1 384 GCCTGTGGTCAAAATCCAGT nbla24434m-R1 385 CTTTGCCTCAGTGGCTCTTC nbla24460m-F1 386 TTTCCAGGAGGTCAGGTTTG nbla24460m-R1 387 CCTTCAGGACACACAGGCTTA nbla24468m-F1 388 TGACAAAGACGCTGAACTGG nbla24468m-R1 389 GGGTTGTCAGAAAGCCTGAG nbla24521m-F1 390 TAATGGGAGTGCTGCCTCTG nbla24521m-R1 391 CATCTTTAAGGCTAACATGC nbla24526m-F1 392 AAGGAGCGCACCAACAGTAT nbla24526m-R1 393 ATAGGGTGGCTCAGGGAAAT nbla24622m-F1 394 GCACTTGGACCTCCCTTGTA nbla24622m-R1 395 GGTCCTGCACATTTCAACAG nbla24672m-F1 396 GGGCAGGACAATAAGACTGC nbla24672m-R1 397 TGTCCACAGCAGACACCCTA nbla24686m-F1 398 AAGAAGGCTCCGAGCTCAAT nbla24686m-R1 399 TCTGTGAGCTCCAGGCAGTA nbla24709m-F1 400 GCAGCATTCTGAGACACAGG nbla24709m-R1 401 GCTGGAGAGACCCAAGGACT nbla24719m-F1 402 CAGGGGATAACCTTCGTCAA nbla24719m-R1 403 AAGCAGCAACGTGGGATAAC nbla24756m-F1 404 ACATTGACAACCCTCCCAAG nbla24756m-R1 405 AAAGCAGCAGCCTCAGAGAA nbla24831m-F1 406 AAACGCTTGAGCTCTTCCAC nbla24831m-R1 407 AGCTCAGCAACCGCTCTAAA nbla24893m-F1 408 AGAGGGGCCAAGGGATATAA nbla24893m-R1 409 TACGAGGGCCTGTTTCAGAT nbla24908m-F1 410 TTCAGAGCATCGAGTTCACG nbla24908m-R1 411 TCATCCTCCTGGGTGAAGTT nbla24972m-F1 412 TCACCAAAACTGGCACAGAG nbla24972m-R1 413 TCGGACTGTGCTGCATTCTA nbla24973m-F1 414 CTGCACACCTCTCAATGCAG nbla24973m-R1 415 GAAGCAGCCCGATGTGTT nbla24986m-F1 416 CAGAGCAGTAACCGTGACCA nbla24986m-R1 417 ACCAGGACGGACACTGTTGT

The results described below were obtained with the genes for which variations in the gene expression level were observed. The genes whose expression levels were decreased notably by NGF depletion (−NGF) were nbla-03267 (SEQ ID NO:21)(−NGF 12 hrs): note 24-48 hrs/−NGF24 hrs to −NGF48 hrs. An increase in expression level was observed under different conditions (−NGF12 hrs) for this gene. Addition of NGF also decreased the expression level. In a similar manner nbla-11589 (SEQ ID NO:64) displayed an increase in the expression level by NGF depletion, but displayed a decrease in the expression level by NGF addition.

The primer sets used to amplify those particular genes are shown in Table 2.

TABLE 2 primer primer sequence primer primer sequence nbla03267m-f CTGCCTTTGAGATGGTGATG nbla03267m-r TGTAGTGCTTTGCATTGTTGG (SEQ ID NO: 124) (SEQ ID NO: 125) nbla11589m-F2 GGAGCTAGCCAAGATGATCG nbla11589m-R2 CTGGCCATCCTAGAGGAGAA (SEQ ID NO: 200) (SEQ ID NO: 201)

As described above, because the superior cervical gangliocytes are known to die (apoptosis) through NGF depletion, the genes that display variations in the expression level are closely connected to the mechanism of apoptosis.

INDUSTRIAL APPLICABILITY

As described above, this invention discloses gene sequences relating to favorable or unfavorable prognosis of neuroblastoma and will enable the provision of their genetic information and the diagnosis of favorable or unfavorable prognosis. 

1. An isolated nucleic acid of SEQ ID NO:21.
 2. A diagnostic agent for the detection of a neurological disease containing an isolated nucleic acid of SEQ ID NO:21. 